The recall covers 142 production lots of Triaminic syrups and 41 lots of Theraflu syrups. Novartis, which produces the medicines, says the defect could allow for the removal the cap without breaking the seal on the bottle. The company says it received four reports of adverse events related to the Triaminic products.
The products were made between May 2010 and December 2011 at a Novartis facility in Nebraska. Novartis shut down that plant in December 2011 after federal inspections found numerous quality-control problems.
Novartis says it believes 97 percent of the inventory has been used, returned, or quarantined.
For a complete list of the recalled products and how to obtain a full refund click here.
Consumers with additional questions can contact the Novartis Consumer Relationship Center at 1-866-553-6742 (available Monday-Saturday 8 a.m. to midnight Eastern Time).